Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial trisomy 3p and partial trisomy loq in humans

Genetika

Volumn 37, Issue 6, 2001, Pages 811-816

  Karamysheva, T V ^a   Matveeva, V G ^a   Shorina, A R ^a   Rubtsov, N B ^a  

^a INSTITUTE OF CYTOLOGY AND GENETICS   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 10; CHROMOSOME 3; CHROMOSOME DELETION; GENE LIBRARY; GENETICS; HUMAN; IN SITU HYBRIDIZATION; MALE; MOSAICISM; MULTIPLE MALFORMATION SYNDROME; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; TRISOMY;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 3; GENE LIBRARY; HUMANS; IN SITU HYBRIDIZATION; MALE; MOSAICISM; POLYMERASE CHAIN REACTION; TRISOMY;

EID: 0035376611     PISSN: 00166758     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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